Gentisic acid

Gentisic acid[1]
Skeletal formula of gentisic acid
Space-filling model of the gentisic acid molecule
Names
Preferred IUPAC name
2,5-Dihydroxybenzoic acid
Other names
DHB
5-Hydroxysalicylic acid
Gentianic acid
Carboxyhydroquinone
2,5-Dioxybenzoic Acid
Hydroquinonecarboxylic acid
Identifiers
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
ECHA InfoCard 100.007.017 Edit this at Wikidata
KEGG
UNII
  • InChI=1S/C7H6O4/c8-4-1-2-6(9)5(3-4)7(10)11/h1-3,8-9H,(H,10,11) checkY
    Key: WXTMDXOMEHJXQO-UHFFFAOYSA-N checkY
  • InChI=1/C7H6O4/c8-4-1-2-6(9)5(3-4)7(10)11/h1-3,8-9H,(H,10,11)
    Key: WXTMDXOMEHJXQO-UHFFFAOYAO
  • O=C(O)c1cc(O)ccc1O
Properties
C7H6O4
Molar mass 154.12 g/mol
Appearance white to yellow powder
Melting point 204 °C (399 °F; 477 K)[3]
Acidity (pKa) 2.97[2]
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
checkY verify (what is checkY☒N ?)

Gentisic acid is a dihydroxybenzoic acid. It is a derivative of benzoic acid and a minor (1%) product of the metabolic break down of aspirin, excreted by the kidneys.[4]

It is also found in the African tree Alchornea cordifolia and in wine.[5]

  1. ^ Gentisic acid - Compound Summary, PubChem.
  2. ^ Haynes, p. 5.91
  3. ^ Haynes, p. 3.190
  4. ^ Levy, G; Tsuchiya, T (1972-08-31). "Salicylate accumulation kinetics in man". New England Journal of Medicine. 287 (9): 430–2. doi:10.1056/NEJM197208312870903. PMID 5044917.
  5. ^ Tian, Rong-Rong; Pan, Qiu-Hong; Zhan, Ji-Cheng; Li, Jing-Ming; Wan, Si-Bao; Zhang, Qing-Hua; Huang, Wei-Dong (2009). "Comparison of Phenolic Acids and Flavan-3-ols During Wine Fermentation of Grapes with Different Harvest Times". Molecules. 14 (2): 827–838. doi:10.3390/molecules14020827. PMC 6253884.